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Cra Training Program Jobs (NOW HIRING)

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Ithaca, NY · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Kansas City, MO · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Bloomington, IL · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Columbus, OH · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Indianapolis, IN · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Marietta, GA · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Las Vegas, NV · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

New York, NY · On-site

$71K - $119K/yr

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

... a CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

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Cra Training Program information

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$25K

$52.4K

$90.5K

How much do cra training program jobs pay per year?

As of Jun 5, 2026, the average yearly pay for cra training program in the United States is $52,360.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $59,500.00 per year, depending on experience, location, and employer.

What is a CRA Training Program?

A CRA (Clinical Research Associate) Training Program is a specialized course designed to prepare individuals for the role of a clinical research associate. These programs cover essential topics such as clinical trial protocols, Good Clinical Practice (GCP) guidelines, regulatory requirements, and monitoring processes. The goal is to equip participants with the knowledge and skills needed to oversee clinical trials, ensure compliance, and maintain data integrity. CRA training programs are often offered by universities, professional organizations, and online platforms to help newcomers enter the clinical research field.

What does a typical week look like for participants in a CRA Training Program?

Participants in a CRA (Clinical Research Associate) Training Program can expect a blend of classroom instruction, practical exercises, and interactive workshops focused on clinical research protocols, regulations, site monitoring, and data management. The week often includes lectures from industry experts, hands-on training with electronic data capture systems, and collaborative problem-solving sessions with peers. Assignments may involve reviewing case studies, preparing monitoring visit reports, and discussing best practices for communication with clinical sites. This structure helps trainees build both technical expertise and essential soft skills required for the CRA role.

What are the key skills and qualifications needed to thrive in a CRA (Clinical Research Associate) Training Program, and why are they important?

To thrive in a CRA Training Program, you need a background in life sciences or healthcare, attention to detail, and a strong understanding of clinical research principles. Familiarity with Good Clinical Practice (GCP) guidelines, data management systems, and regulatory documentation is typically required. Strong organizational skills, effective communication, and the ability to work independently set successful candidates apart. These skills ensure accurate trial monitoring, regulatory compliance, and effective collaboration with research teams.
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What cities are hiring for Cra Training Program jobs? Cities with the most Cra Training Program job openings:
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Infographic showing various Cra Training Program job openings in the United States as of May 2026, with employment types broken down into 3% Locum Tenens, 4% Internship, 3% Full Time, 89% Contract, and 1% Summer. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $52,360 per year, or $25.2 per hour.
CRA 1, IQVIA Biotech

CRA 1, IQVIA Biotech

IQVIA

San Francisco, CA

$71K - $119K/yr

Full-time

Posted 19 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

52nd of 203 rated it services


Job description

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring highquality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits-including site selection, initiation, routine monitoring, and closeout visits-to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address sitelevel challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or startup activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

  • Bachelor's degree required; a scientific or healthcare discipline is preferred.
  • 6 months -2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
  • Basic knowledge of clinical research regulations (GCP/ICH).
  • Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $119,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US